Production of cell wall degrading enzymes and antibiotic by Pseudomonads for assessing their biocontrol potential
203 / 167
Keywords:
Biocontrol, Chitinase, 2, 4-DAPG, Lipase, Protease, PseudomonasAbstract
A comprehensive study on bio-control efficacy of different Pseudomonas species was made in terms of cell wall degrading enzymes, viz. chitinase, lipase, protease and antibiotic 2, 4- diacetylphloroglucinol (2,4- DAPG) production abilities in respect to changing temperatures and pH. Observations revealed that all the isolates of Pseudomonas spp. under study produced all the three cell wall degrading enzymes and 2,4- DAPG significantly. However, the isolates PS-11 and PS-30 exhibited maximum enzyme producing abilities. Moreover, PS-11 could be considered to be the maximum heat tolerant among the isolates as it maintain remarkable sustainability even at 55° C in the ability to produce enzymes with minimum losses in activities 0.1026 to 0.718 in chitinase, 3.1167 to 2.1794 in lipase and 0.5827 to 0.4075 in protease activities due to rise of temperature from 45° C to 55° C. In pH variation studied at 35°C, it was observed that chitinase, lipase and protease production abilities of most of the isolates of Pseudomonas spp. were maximum at pH value of 6.5 and decreased on further lowering to 5.5 or rising to pH 8.5. PS-30 recorded the highest production of 2,4-DAPG (767.37 μg/ml) at 30° C and pH 6.5.Downloads
References
Al-Saleh A A and Zahran A S. 1999. Synthesis of extracellular lipase by a strain of Pseudomonas fluorescens isolated from raw camel milk. Food Microbiology 16: 149–56. DOI: https://doi.org/10.1006/fmic.1998.0227
Dunne C, Crowley J J, Moe¨nne-Loccoz Y, Dowling D N, de Bruijn F Jand O’Gara F. 1997. Biological control of Pythium ultimum by Stenotrophomonas maltophilia W81 is mediated by an extracellular proteolytic activity. Microbiology 143: 3921–31. DOI: https://doi.org/10.1099/00221287-143-12-3921
Euzeby J P. 1997. List of bacterial names with standing in nomenclature: A folder available on the Internet. International Journal of Systematic Bacteriology 47: 590–2. DOI: https://doi.org/10.1099/00207713-47-2-590
Gupta A, Singh R, Khare S K, and Gupta M N. 2002. An extracellular alkaline lipase from Enterobacter aerogenes. Indian Journal of Microbiology 42: 263–5.
Kathiravan T, Marykala J, Sundaramanickam A, Kumaresan S and Balasubramanian T. 2012. Studies on nutritional requirements of Pseudomonas aeruginosa for lipase production. Advances in Applied Science Research 3: 591–8.
Mallick S A, Kumari P, Gupta Mand Gupta S. 2015. Effect of Alternaria blight infection on biochemical parameters, quantity and quality of oil of mustard genotypes. Indian Journal of Plant Physiology 20(4): 310–6. DOI: https://doi.org/10.1007/s40502-015-0178-z
Miller G L.1959. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Analytical Chemistry 37: 426–8. DOI: https://doi.org/10.1021/ac60147a030
Mondal S, Baksi S, Koris A and Vatai G. 2016. Journey of enzymes in entomopathogenic fungi. Pacific Science Review A: Natural Science and Engineering 18: 85–99. DOI: https://doi.org/10.1016/j.psra.2016.10.001
Naseby D C, Pascual J A and Lynch J M. 2000. Effect of biocontrol strains of Trichoderma on plant growth, Pythiumultimum populations, soil microbial communities and soil enzyme activities. Journal of Applied Microbiology 88: 161–9. DOI: https://doi.org/10.1046/j.1365-2672.2000.00939.x
Prasad R and Lallu. 2006. Management of Alternaria blight of mustard with combination of chemical and botanicals. Annals of Plant Protection Sciences 14: 400–03.
Rosales A M, Thomashow L, Cook R J and Mew T W. 1995. Isolation and identification of antifungal metabolites produced by rice-associated antagonistic Pseudomonas spp. Phytopathology 85: 1028–32. DOI: https://doi.org/10.1094/Phyto-85-1028
Rousk J and Baath E. 2011. Growth of saprotrophic fungi and bacteria in soil.FEMS Microbiology Ecology 78: 17–30. DOI: https://doi.org/10.1111/j.1574-6941.2011.01106.x
Sacherer P, Defago G and Haas D. 1994. Extracellular protease and phospholipase C arecontrolled by the global regulatory gene gacA in the biocontrol strain Pseudomonas fluorescens CHAO. FEMS Microbiology Letters 116: 115–60. DOI: https://doi.org/10.1111/j.1574-6968.1994.tb06694.x
Senol M, Nadaroglu H, Dikbas N and Kotan R. 2014. Purification of Chitinaseenzymes from Bacillus subtilis bacteria TV-125, investigation of kinetic properties and antifungal activity against Fusarium culmorum.Annalsof Clinical Microbiology and Antimicrobials 13: 35. DOI: https://doi.org/10.1186/s12941-014-0035-3
Sharma D. 2014. ‘Biochemical characterization of fluorescent pseudomonads isolated from Jammu soils’. MSc (Biochemistry) thesis, Chatha, Jammu and Kashmir, India.
Sharma D, Gupta M, Gupta S, Kashyap P L, Zargar S M and Mallick S A. 2018. Antibiotic gene specific characterization and ARDRA analysis of native isolates of Pseudomonas spp. from Jammu, India. Indian Phytopathology 71: 225–33. DOI: https://doi.org/10.1007/s42360-018-0028-9
Vasantha S T and Subramanian A T. 2012. Optimization of cultural conditions for the production of an extra-cellular protease by Pseudomonas species. International Current Pharmaceutical Journal 2: 1–6. DOI: https://doi.org/10.3329/icpj.v2i1.12870
Weller D M. 2007. Pseudomonas biocontrol agents of soilborne pathogens: Looking back over 30 years. Phytopathology 97: 250–6. DOI: https://doi.org/10.1094/PHYTO-97-2-0250
Downloads
Submitted
Published
Issue
Section
License
Copyright (c) 2019 The Indian Journal of Agricultural Sciences

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
The copyright of the articles published in The Indian Journal of Agricultural Sciences is vested with the Indian Council of Agricultural Research, which reserves the right to enter into any agreement with any organization in India or abroad, for reprography, photocopying, storage and dissemination of information. The Council has no objection to using the material, provided the information is not being utilized for commercial purposes and wherever the information is being used, proper credit is given to ICAR.